Canonical Allele Identifier: CA936881004
Gene: PRR5L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350165_36350210del , CM000673.2:g.36350165_36350210del GRCh38
NC_000011.9:g.36371715_36371760del , CM000673.1:g.36371715_36371760del GRCh37
NC_000011.8:g.36328291_36328336del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50832_-125-50787del MANE Select ENSP00000435050.1:n.-125-50832_-125-50787...
ENST00000527172.5:c.-291-43681_-291-43636del ENSP00000433708.1:n.-291-43681_-291-43636...
ENST00000529034.5:n.152-50832_152-50787del
ENST00000530639.5:c.-125-50832_-125-50787del ENSP00000435050.1:n.-125-50832_-125-50787...
ENST00000532121.5:c.-126+100_-126+145del ENSP00000433893.1:n.-126+100_-126+145del
NM_001160167.1:c.-125-50832_-125-50787del NP_001153639.1:n.-125-50832_-125-50787del...
NM_001160167.2:c.-125-50832_-125-50787del MANE Select NP_001153639.1:n.-125-50832_-125-50787del...